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CAS

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35896-46-9

4-nitrobenzyl trifluoromethanesulfinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 35896-46-9 Structure

  • Basic information

    1. Product Name: 4-nitrobenzyl trifluoromethanesulfinate
    2. Synonyms:
    3. CAS NO:35896-46-9
    4. Molecular Formula:
    5. Molecular Weight: 269.201
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35896-46-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-nitrobenzyl trifluoromethanesulfinate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-nitrobenzyl trifluoromethanesulfinate(35896-46-9)
    11. EPA Substance Registry System: 4-nitrobenzyl trifluoromethanesulfinate(35896-46-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 35896-46-9(Hazardous Substances Data)

35896-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35896-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,9 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35896-46:
(7*3)+(6*5)+(5*8)+(4*9)+(3*6)+(2*4)+(1*6)=159
159 % 10 = 9
So 35896-46-9 is a valid CAS Registry Number.

35896-46-9Downstream Products

35896-46-9Relevant articles and documents

Synthesis of Difluoromethanesulfinate Esters by the Difluoromethanesulfinylation of Alcohols

Sumii, Yuji,Sasaki, Kenta,Matsubara, Okiya,Shibata, Norio

, p. 2777 - 2782 (2021)

Herein, we report the first synthesis of difluoromethanesulfinate esters via the direct difluoromethanesulfinylation of alcohols with HCF2SO2Na/Ph2P(O)Cl. Primary, secondary, and tertiary alcohols were converted to the corresponding difluoromethanesulfinate esters in good to excellent yields under mild conditions. The late-stage functionalization of complexed biologically active natural products was also demonstrated. The method was extended to the trifluoromethanesulfinylation of alcohols using CF3SO2Na in the presence of a catalytic amount of Me3SiCl to provide trifluoromethanesulfinate esters.

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